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rs1064796540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
ChromosomeX
Position22245380
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064796540
dbSNP (old)rs1064796540
ClinGenrs1064796540
ebirs1064796540
HLIrs1064796540
Exacrs1064796540
Gnomadrs1064796540
Varsomers1064796540
LitVarrs1064796540
Maprs1064796540
PheGenIrs1064796540
Biobankrs1064796540
1000 genomesrs1064796540
hgdprs1064796540
ensemblrs1064796540
gopubmedrs1064796540
geneviewrs1064796540
scholarrs1064796540
googlers1064796540
pharmgkbrs1064796540
gwascentralrs1064796540
openSNPrs1064796540
23andMers1064796540
23andMe allrs1064796540
SNPshotrs1064796540
SNPdbers1064796540
MSV3drs1064796540
GWAS Ctlgrs1064796540
Max Magnitude0
ClinVar
Risk rs1064796540(-;-)
Alt rs1064796540(-;-)
Reference Rs1064796540(AA;AA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22263497_22263498delAA
CLNSRC
CLNACC RCV000479229.1,